US8173360B2ExpiredUtilityA1
Cell death inhibitor
Est. expiryApr 26, 2022(expired)· nominal 20-yr term from priority
A61P 43/00A61P 9/00A61P 9/04A61P 9/10A61P 9/12A61P 37/06A61P 35/00A61P 25/28A61P 31/00A61P 3/10A61P 19/02A61P 13/12G01N 2333/52C07D 279/08A61P 1/00A61P 11/00G01N 2500/02C07D 417/04A61K 31/5415A61P 1/16A61K 31/00
54
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3
Claims
Abstract
The cell death inhibitor comprising a substance capable of binding to macrophage migration inhibitory factor is useful as a preventive/therapeutic agent for, e.g., heart diseases, neurodegenerative diseases, cerebrovascular diseases, central nervous infections, traumatic diseases, demyelinating diseases, bone/joint diseases, kidney diseases, liver diseases, myelodysplastic diseases, arteriosclerosis, diabetes, pulmonary hypertension, sepsis, inflammatory bowel diseases, autoimmune diseases, failure accompanying rejection in organ transplantation, AIDS, cancer, etc.
Claims
exact text as granted — not AI-modified1. A method of screening a test compound as a cell death inhibitor, the method comprising determining whether the test compound binds to macrophage migration inhibitory factor, and determining whether the test compound promotes expression of a gene under control of an antioxidant response element selected from the group consisting of Heme oxygenase-1, Liver glutathione S-transferase Ya subunit, Liver glutathione S-transferase Yc subunit, Glutathione S-transferase Yb subunit, Glutathione S-transferase Yc1 subunit, Gamma-glutamylcysteine synthetase, NAD(P)H: quinone reductase, UDP-glucuronosyltransferase, exon 1, Bilirunin-specific UDP-glucuronosyltransferase and NAD(P)H-menadione oxidereductase, wherein binding to macrophage migration inhibitory factor and promoting expression of the gene under control of an antioxidant response element indicates that the test compound is a cell death inhibitor.
2. The screening method according to claim 1 , wherein (i) macrophage migration inhibitory factor is mixed with a labeled compound capable of binding to macrophage migration inhibitory factor; and (ii) the test compound and macrophage migration inhibitory factor are mixed with the labeled compound capable of binding to macrophage migration inhibitory factor; and the binding amounts of the labeled compounds bound to the macrophage migration inhibitory factor are measured in each case, and comparison is made therebetween, to thereby determine whether the test compound binds to macrophage migration inhibitory factor.
3. The screening method according to claim 1 , wherein the gene under control of an antioxidant response element is heme oxygenase-1.Cited by (0)
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